hypertrophic cardiomyopathy Gene Set

Dataset GWASdb SNP-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description An intrinsic cardiomyopathy that is characterized by abnormal thickening (hypertrophy) of the heart without any obvious cause. (Human Disease Ontology, DOID_11984)
External Link http://jjwanglab.org/gwasdb/gwasdb2/gwasdb2/go_trait/HP:0001639
Similar Terms
Downloads & Tools

Genes

5 genes associated with the hypertrophic cardiomyopathy phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

Symbol Name Standardized Value
COL17A1 collagen, type XVII, alpha 1 1.21853
ESRRG estrogen-related receptor gamma 1.15352
RAF1 Raf-1 proto-oncogene, serine/threonine kinase 1.0674
FGF1 fibroblast growth factor 1 (acidic) 1.05869
PHF11 PHD finger protein 11 0.919744